Salt-induced gelation of nonionic sucrose ester dispersions

Abstract

The dispersions of nonionic sucrose ester surfactants in water exhibit a highly negative zeta-potential, though its origin remains controversial. The addition of electrolytes to these dispersions may influence their zeta-potential, thus potentially affecting their physicochemical properties. The electrolyte- and pH- driven gelation of aqueous dispersions of commercial sucrose stearate (S970) containing ca. 1:1 monoesters and diesters was studied using optical microscopy, rheological and zeta-potential measurements, and small-angle X-ray scattering techniques. At low electrolyte concentrations and pH $\gtrapprox$ 5, 0.5-5 wt. % S970 dispersions exhibited low viscosities and behaved as freely flowing liquids. The addition of electrolytes of low concentrations, e.g. 9 mM NaCl or 1.5 mM MgCl$_2$, induced the formation of a non-flowing gels. This sol-gel transition occurred due to the partial screening of the diesters particles charge, allowing the formation of an attractive gel network, spanning across the dispersion volume. Complete charge screening, however, led to a gel-sol transition and phase separation. Gel formation was observed also by pH variation without electrolyte addition, whereas the addition of free fatty acids had negligible impact on dispersion properties. These findings support the hypothesis that the negative charge in sucrose ester dispersions arises from hydroxyl anions adsorption on particles surfaces. Gels were formed using just 1.3 wt. % surfactant, and the critical electrolyte concentration for gelation was found to scale approximately with the square of the cation charge, in agreement with the low surface charge density theory. The biodegradable sucrose esters gels offer a sustainable alternative for structuring personal and home care products, replacing the wormlike micelles of synthetic surfactants typically used at much higher surfactant and salt concentrations.